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Origin and Spread of Spliceosomal Introns: Insights from the Fungal Clade Zymoseptoria
Spliceosomal introns are a key feature of eukaryote genome architecture and have been proposed to originate from selfish group II introns from an endosymbiotic bacterium, that is, the ancestor of mitochondria. However, the mechanisms underlying the wide spread of spliceosomal introns across eukaryot...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5647799/ https://www.ncbi.nlm.nih.gov/pubmed/29048531 http://dx.doi.org/10.1093/gbe/evx211 |
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author | Wu, Baojun Macielog, Allison I. Hao, Weilong |
author_facet | Wu, Baojun Macielog, Allison I. Hao, Weilong |
author_sort | Wu, Baojun |
collection | PubMed |
description | Spliceosomal introns are a key feature of eukaryote genome architecture and have been proposed to originate from selfish group II introns from an endosymbiotic bacterium, that is, the ancestor of mitochondria. However, the mechanisms underlying the wide spread of spliceosomal introns across eukaryotic genomes have been obscure. In this study, we characterize the dynamic evolution of spliceosomal introns in the fungal genus Zymoseptoria at different evolutionary scales, that is, within a genome, among conspecific strains within species, and between different species. Within the genome, spliceosomal introns can proliferate in unrelated genes and intergenic regions. Among conspecific strains, spliceosomal introns undergo rapid turnover (gains and losses) and frequent sequence exchange between geographically distinct strains. Furthermore, spliceosomal introns could undergo introgression between distinct species, which can further promote intron invasion and proliferation. The dynamic invasion and proliferation processes of spliceosomal introns resemble the life cycles of mobile selfish (group I/II) introns, and these intron movements, at least in part, account for the dramatic processes of intron gain and intron loss during eukaryotic evolution. |
format | Online Article Text |
id | pubmed-5647799 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-56477992017-10-25 Origin and Spread of Spliceosomal Introns: Insights from the Fungal Clade Zymoseptoria Wu, Baojun Macielog, Allison I. Hao, Weilong Genome Biol Evol Research Article Spliceosomal introns are a key feature of eukaryote genome architecture and have been proposed to originate from selfish group II introns from an endosymbiotic bacterium, that is, the ancestor of mitochondria. However, the mechanisms underlying the wide spread of spliceosomal introns across eukaryotic genomes have been obscure. In this study, we characterize the dynamic evolution of spliceosomal introns in the fungal genus Zymoseptoria at different evolutionary scales, that is, within a genome, among conspecific strains within species, and between different species. Within the genome, spliceosomal introns can proliferate in unrelated genes and intergenic regions. Among conspecific strains, spliceosomal introns undergo rapid turnover (gains and losses) and frequent sequence exchange between geographically distinct strains. Furthermore, spliceosomal introns could undergo introgression between distinct species, which can further promote intron invasion and proliferation. The dynamic invasion and proliferation processes of spliceosomal introns resemble the life cycles of mobile selfish (group I/II) introns, and these intron movements, at least in part, account for the dramatic processes of intron gain and intron loss during eukaryotic evolution. Oxford University Press 2017-10-03 /pmc/articles/PMC5647799/ /pubmed/29048531 http://dx.doi.org/10.1093/gbe/evx211 Text en © The Author 2017. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Research Article Wu, Baojun Macielog, Allison I. Hao, Weilong Origin and Spread of Spliceosomal Introns: Insights from the Fungal Clade Zymoseptoria |
title | Origin and Spread of Spliceosomal Introns: Insights from the Fungal Clade Zymoseptoria |
title_full | Origin and Spread of Spliceosomal Introns: Insights from the Fungal Clade Zymoseptoria |
title_fullStr | Origin and Spread of Spliceosomal Introns: Insights from the Fungal Clade Zymoseptoria |
title_full_unstemmed | Origin and Spread of Spliceosomal Introns: Insights from the Fungal Clade Zymoseptoria |
title_short | Origin and Spread of Spliceosomal Introns: Insights from the Fungal Clade Zymoseptoria |
title_sort | origin and spread of spliceosomal introns: insights from the fungal clade zymoseptoria |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5647799/ https://www.ncbi.nlm.nih.gov/pubmed/29048531 http://dx.doi.org/10.1093/gbe/evx211 |
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